Canonical Allele Identifier: CA995878693
Gene: AKT2 HGNC NCBI

Linked Data

dbSNP Id: rs2077497678

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.40285361_40285380dup , CM000681.2:g.40285361_40285380dup GRCh38
NC_000019.9:g.40791268_40791287dup , CM000681.1:g.40791268_40791287dup GRCh37
NC_000019.8:g.45483108_45483127dup NCBI36
NG_012038.2:g.4979_4998dup

Transcript Alleles

HGVS Amino-acid change
ENST00000392038.6:c.-284_-265dup ENSP00000375892.2:n.-284_-265dup
ENST00000424901.5:c.-284_-265dup ENSP00000399532.2:n.-284_-265dup
ENST00000578123.5:c.-85+68_-85+87dup ENSP00000462022.1:n.-85+68_-85+87dup
NM_001243027.2:c.-433_-414dup NP_001229956.1:n.-433_-414dup
NM_001243028.2:c.-340_-321dup NP_001229957.1:n.-340_-321dup
NM_001626.5:c.-284_-265dup NP_001617.1:n.-284_-265dup
XM_011526620.1:c.-85+68_-85+87dup XP_011524922.1:n.-85+68_-85+87dup